Canonical Allele Identifier: CA351496597

Gene: RAF1 MKRN2

Linked Data

• MyVariant Identifiers: chr3:g.12626381T>A (hg19) ; chr3:g.12584882T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12584882T>A , CM000665.2:g.12584882T>A	GRCh38
NC_000003.11:g.12626381T>A , CM000665.1:g.12626381T>A	GRCh37
NC_000003.10:g.12601381T>A	NCBI36
NG_007467.1:g.84298A>T , LRG_413:g.84298A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423275.6:c.*1433A>T (RAF1)	ENSP00000401088.1:n.*1433A>T
ENST00000432427.3:c.1085A>T (RAF1)
ENST00000460610.2:n.6080A>T (RAF1)
ENST00000471449.2:n.578A>T (RAF1)
ENST00000475353.2:n.4048A>T (RAF1)
ENST00000684903.1:c.*1445A>T (RAF1)	ENSP00000508612.1:n.*1445A>T
ENST00000685348.1:c.*1479A>T (RAF1)	ENSP00000510285.1:n.*1479A>T
ENST00000685437.1:c.1669A>T (RAF1)	ENSP00000508794.1:p.Lys557Ter
ENST00000685653.1:c.1768A>T (RAF1)	ENSP00000509968.1:p.Lys590Ter
ENST00000685697.1:n.2503A>T (RAF1)
ENST00000685738.1:c.*732A>T (RAF1)	ENSP00000510156.1:n.*732A>T
ENST00000686409.1:n.5177A>T (RAF1)
ENST00000686455.1:n.4489A>T (RAF1)
ENST00000686762.1:c.*327A>T (RAF1)	ENSP00000509767.1:n.*327A>T
ENST00000687257.1:n.4222A>T (RAF1)
ENST00000687326.1:c.*3060A>T (RAF1)	ENSP00000509665.1:n.*3060A>T
ENST00000687505.1:n.1886A>T (RAF1)
ENST00000687923.1:c.1657A>T (RAF1)	ENSP00000510255.1:p.Lys553Ter
ENST00000688269.1:n.2364A>T (RAF1)
ENST00000688444.1:n.3885A>T (RAF1)
ENST00000688543.1:c.1669A>T (RAF1)	ENSP00000509612.1:p.Lys557Ter
ENST00000688625.1:c.*3137A>T (RAF1)	ENSP00000509522.1:n.*3137A>T
ENST00000688803.1:n.3196A>T (RAF1)
ENST00000689097.1:c.*1445A>T (RAF1)	ENSP00000509756.1:n.*1445A>T
ENST00000689389.1:c.1591A>T (RAF1)	ENSP00000510213.1:p.Lys531Ter
ENST00000689418.1:c.*3663A>T (RAF1)	ENSP00000509467.1:n.*3663A>T
ENST00000689540.1:n.4136A>T (RAF1)
ENST00000689876.1:c.*317A>T (RAF1)	ENSP00000508535.1:n.*317A>T
ENST00000689914.1:c.*702A>T (RAF1)	ENSP00000509847.1:n.*702A>T
ENST00000690397.1:c.1657A>T (RAF1)	ENSP00000508730.1:p.Lys553Ter
ENST00000690460.1:c.1756A>T (RAF1)	ENSP00000509106.1:p.Lys586Ter
ENST00000690585.1:c.494A>T (RAF1)
ENST00000690625.1:n.2804A>T (RAF1)
ENST00000691396.1:c.*1640A>T (RAF1)	ENSP00000510712.1:n.*1640A>T
ENST00000691643.1:n.2821A>T (RAF1)
ENST00000691724.1:c.*725A>T (RAF1)	ENSP00000509255.1:n.*725A>T
ENST00000691779.1:c.*1346A>T (RAF1)	ENSP00000508592.1:n.*1346A>T
ENST00000691888.1:c.642A>T (RAF1)
ENST00000691899.1:c.1768A>T (RAF1)	ENSP00000508763.1:p.Lys590Ter
ENST00000692069.1:n.4692A>T (RAF1)
ENST00000692093.1:c.1669A>T (RAF1)	ENSP00000509669.1:p.Lys557Ter
ENST00000692311.1:n.2592A>T (RAF1)
ENST00000692558.1:n.4351A>T (RAF1)
ENST00000692773.1:c.*1505A>T (RAF1)	ENSP00000509055.1:n.*1505A>T
ENST00000692830.1:c.*1513A>T (RAF1)	ENSP00000509461.1:n.*1513A>T
ENST00000693312.1:c.1543A>T (RAF1)	ENSP00000508686.1:p.Lys515Ter
ENST00000693664.1:c.*219A>T (RAF1)	ENSP00000509614.1:n.*219A>T
ENST00000693705.1:c.*1147A>T (RAF1)	ENSP00000510697.1:n.*1147A>T
ENST00000251849.9:c.1768A>T (RAF1) MANE Select	ENSP00000251849.4:p.Lys590Ter
ENST00000442415.7:c.1828A>T (RAF1)	ENSP00000401888.2:p.Lys610Ter
ENST00000676541.1:c.*2629T>A (MKRN2)	ENSP00000503730.1:n.*2629T>A
ENST00000677142.1:c.*2629T>A (MKRN2)	ENSP00000504455.1:n.*2629T>A
ENST00000677816.1:c.*1184T>A (MKRN2)	ENSP00000502893.1:n.*1184T>A
ENST00000677941.1:n.2692T>A (MKRN2)
ENST00000251849.8:c.1768A>T (RAF1)	ENSP00000251849.4:p.Lys590Ter
ENST00000423275.5:c.*1445A>T (RAF1)	ENSP00000401088.1:n.*1445A>T
ENST00000432427.2:c.1405A>T (RAF1)	ENSP00000398591.2:p.Lys469Ter
ENST00000442415.6:c.1828A>T (RAF1)	ENSP00000401888.2:p.Lys610Ter
ENST00000471449.1:n.457A>T (RAF1)
NM_002880.3:c.1768A>T , LRG_413t1:c.1768A>T (RAF1)	NP_002871.1:p.Lys590Ter
XM_005265355.1:c.1768A>T (RAF1)	XP_005265412.1:p.Lys590Ter
XM_005265357.1:c.1669A>T (RAF1)	XP_005265414.1:p.Lys557Ter
XM_005265358.3:c.1525A>T (RAF1)	XP_005265415.1:p.Lys509Ter
XM_005265359.3:c.1426A>T (RAF1)	XP_005265416.1:p.Lys476Ter
XM_011533974.1:c.1768A>T (RAF1)	XP_011532276.1:p.Lys590Ter
XM_011533975.1:c.1525A>T (RAF1)	XP_011532277.1:p.Lys509Ter
NM_001354689.1:c.1828A>T (RAF1)	NP_001341618.1:p.Lys610Ter
NM_001354690.1:c.1768A>T (RAF1)	NP_001341619.1:p.Lys590Ter
NM_001354691.1:c.1525A>T (RAF1)	NP_001341620.1:p.Lys509Ter
NM_001354692.1:c.1525A>T (RAF1)	NP_001341621.1:p.Lys509Ter
NM_001354693.1:c.1669A>T (RAF1)	NP_001341622.1:p.Lys557Ter
NM_001354694.1:c.1585A>T (RAF1)	NP_001341623.1:p.Lys529Ter
NM_001354695.1:c.1426A>T (RAF1)	NP_001341624.1:p.Lys476Ter
NR_148940.1:n.2296A>T (RAF1)
NR_148941.1:n.2242A>T (RAF1)
NR_148942.1:n.2181A>T (RAF1)
XM_011533974.3:c.1768A>T (RAF1)	XP_011532276.1:p.Lys590Ter
XM_017006966.1:c.1669A>T (RAF1)	XP_016862455.1:p.Lys557Ter
NM_001354689.3:c.1828A>T (RAF1)	NP_001341618.1:p.Lys610Ter
NM_001354690.2:c.1768A>T (RAF1)	NP_001341619.1:p.Lys590Ter
NM_001354691.2:c.1525A>T (RAF1)	NP_001341620.1:p.Lys509Ter
NM_001354692.2:c.1525A>T (RAF1)	NP_001341621.1:p.Lys509Ter
NM_001354693.2:c.1669A>T (RAF1)	NP_001341622.1:p.Lys557Ter
NM_001354694.2:c.1585A>T (RAF1)	NP_001341623.1:p.Lys529Ter
NM_001354695.2:c.1426A>T (RAF1)	NP_001341624.1:p.Lys476Ter
NR_148940.2:n.2212A>T (RAF1)
NR_148941.2:n.2158A>T (RAF1)
NR_148942.2:n.2097A>T (RAF1)
NM_001354690.3:c.1768A>T (RAF1)	NP_001341619.1:p.Lys590Ter
NM_001354691.3:c.1525A>T (RAF1)	NP_001341620.1:p.Lys509Ter
NM_001354692.3:c.1525A>T (RAF1)	NP_001341621.1:p.Lys509Ter
NM_001354693.3:c.1669A>T (RAF1)	NP_001341622.1:p.Lys557Ter
NM_001354694.3:c.1585A>T (RAF1)	NP_001341623.1:p.Lys529Ter
NM_001354695.3:c.1426A>T (RAF1)	NP_001341624.1:p.Lys476Ter
NM_002880.4:c.1768A>T (RAF1) MANE Select	NP_002871.1:p.Lys590Ter
NR_148940.3:n.2212A>T (RAF1)
NR_148941.3:n.2158A>T (RAF1)
NR_148942.3:n.2097A>T (RAF1)